Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3309097011 | Syndromic hypoplasia of orbital border (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3309098018 | Syndromic orbital border hypoplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3309099014 | Urrets Zavalia syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3309100018 | Syndromic hypoplasia of orbital border | en | Synonym | Active | Case insensitive | SNOMED CT core |
3309101019 | Syndromic orbital border hypoplasia is a rare disorder observed in two families to date with characteristics of agenesis of the orbital margin, varying defects of the lacrimal passages, hypoplasia of the palpebral skin and tarsal plates and atresia of the nasolacrimal duct. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set